CA1085094A - Vinyl halide polymerization in internally cooled reactor - Google Patents

Vinyl halide polymerization in internally cooled reactor

Info

Publication number: CA1085094A
Authority: CA; Canada
Prior art keywords: process according; reactor; compounds; group; chosen
Prior art date: 1977-03-08
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA298,530A

Other languages

English (en)

French (fr)

Inventor

Boris Englin

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Orica Ltd

Original Assignee

ICI Australia Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1977-03-08

Filing date

1978-03-08

Publication date

1980-09-02

1978-03-08 Application filed by ICI Australia Ltd filed Critical ICI Australia Ltd

1980-09-02 Application granted granted Critical

1980-09-02 Publication of CA1085094A publication Critical patent/CA1085094A/en

Status Expired legal-status Critical Current

Links

-1 Vinyl halide Chemical class 0.000 title claims abstract description 21
229920002554 vinyl polymer Polymers 0.000 title claims abstract description 15
238000006116 polymerization reaction Methods 0.000 title claims abstract description 11
238000000034 method Methods 0.000 claims abstract description 35
230000008569 process Effects 0.000 claims abstract description 33
150000001875 compounds Chemical class 0.000 claims abstract description 31
239000000178 monomer Substances 0.000 claims abstract description 28
239000011248 coating agent Substances 0.000 claims abstract description 18
238000000576 coating method Methods 0.000 claims abstract description 18
239000008199 coating composition Substances 0.000 claims abstract description 15
239000000203 mixture Substances 0.000 claims abstract description 12
150000004982 aromatic amines Chemical class 0.000 claims abstract description 7
150000001491 aromatic compounds Chemical class 0.000 claims abstract description 6
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 6
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims abstract description 6
239000001301 oxygen Substances 0.000 claims abstract description 6
229910052760 oxygen Inorganic materials 0.000 claims abstract description 6
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 22
WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 claims description 20
239000006185 dispersion Substances 0.000 claims description 15
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 14
229960004337 hydroquinone Drugs 0.000 claims description 11
ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 claims description 10
229940079877 pyrogallol Drugs 0.000 claims description 10
SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 claims description 10
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 9
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 9
HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 9
239000007788 liquid Substances 0.000 claims description 8
239000003513 alkali Substances 0.000 claims description 7
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 5
229960004050 aminobenzoic acid Drugs 0.000 claims description 5
DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims description 4
RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 claims description 4
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 4
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 3
WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 claims description 2
XESZUVZBAMCAEJ-UHFFFAOYSA-N 4-tert-butylcatechol Chemical compound CC(C)(C)C1=CC=C(O)C(O)=C1 XESZUVZBAMCAEJ-UHFFFAOYSA-N 0.000 claims description 2
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical class [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 2
AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 claims description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
230000001464 adherent effect Effects 0.000 claims description 2
229910052783 alkali metal Inorganic materials 0.000 claims description 2
229910000288 alkali metal carbonate Inorganic materials 0.000 claims description 2
150000008041 alkali metal carbonates Chemical class 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
150000001896 cresols Chemical class 0.000 claims description 2
125000005265 dialkylamine group Chemical group 0.000 claims description 2
229940035422 diphenylamine Drugs 0.000 claims description 2
239000007800 oxidant agent Substances 0.000 claims description 2
229950000688 phenothiazine Drugs 0.000 claims description 2
OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 claims description 2
150000003142 primary aromatic amines Chemical class 0.000 claims description 2
150000003336 secondary aromatic amines Chemical class 0.000 claims description 2
239000000243 solution Substances 0.000 claims 2
235000011114 ammonium hydroxide Nutrition 0.000 claims 1
239000007864 aqueous solution Substances 0.000 claims 1
230000015572 biosynthetic process Effects 0.000 abstract description 5
150000004053 quinones Chemical class 0.000 abstract description 3
125000001931 aliphatic group Chemical group 0.000 abstract 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 20
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
239000002904 solvent Substances 0.000 description 10
238000006243 chemical reaction Methods 0.000 description 9
150000001412 amines Chemical class 0.000 description 7
239000003999 initiator Substances 0.000 description 7
229920000642 polymer Polymers 0.000 description 7
239000000047 product Substances 0.000 description 7
238000004140 cleaning Methods 0.000 description 6
239000003995 emulsifying agent Substances 0.000 description 6
239000010408 film Substances 0.000 description 5
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
239000004372 Polyvinyl alcohol Substances 0.000 description 4
239000007900 aqueous suspension Substances 0.000 description 4
239000007795 chemical reaction product Substances 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
238000010438 heat treatment Methods 0.000 description 4
229920002451 polyvinyl alcohol Polymers 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
239000000463 material Substances 0.000 description 3
238000002156 mixing Methods 0.000 description 3
229920002689 polyvinyl acetate Polymers 0.000 description 3
229920000915 polyvinyl chloride Polymers 0.000 description 3
239000004800 polyvinyl chloride Substances 0.000 description 3
239000002244 precipitate Substances 0.000 description 3
239000010409 thin film Substances 0.000 description 3
238000012546 transfer Methods 0.000 description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
108010010803 Gelatin Proteins 0.000 description 2
YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
150000004054 benzoquinones Chemical class 0.000 description 2
238000007664 blowing Methods 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
238000011161 development Methods 0.000 description 2
230000018109 developmental process Effects 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000007789 gas Substances 0.000 description 2
239000008273 gelatin Substances 0.000 description 2
229920000159 gelatin Polymers 0.000 description 2
235000019322 gelatine Nutrition 0.000 description 2
235000011852 gelatine desserts Nutrition 0.000 description 2
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
239000002245 particle Substances 0.000 description 2
150000002978 peroxides Chemical class 0.000 description 2
239000011118 polyvinyl acetate Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
239000002002 slurry Substances 0.000 description 2
HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 2
238000005507 spraying Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
238000005406 washing Methods 0.000 description 2
PVCVRLMCLUQGBT-UHFFFAOYSA-N (1-tert-butylcyclohexyl) (1-tert-butylcyclohexyl)oxycarbonyloxy carbonate Chemical compound C1CCCCC1(C(C)(C)C)OC(=O)OOC(=O)OC1(C(C)(C)C)CCCCC1 PVCVRLMCLUQGBT-UHFFFAOYSA-N 0.000 description 1
BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 1
FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 1
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
VXVUDUCBEZFQGY-UHFFFAOYSA-N 4,4-dimethylpentanenitrile Chemical compound CC(C)(C)CCC#N VXVUDUCBEZFQGY-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
241000972773 Aulopiformes Species 0.000 description 1
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
239000004641 Diallyl-phthalate Substances 0.000 description 1
IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 1
239000004150 EU approved colour Substances 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
239000006057 Non-nutritive feed additive Substances 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
229920001800 Shellac Polymers 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
238000009825 accumulation Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
239000013543 active substance Substances 0.000 description 1
238000013019 agitation Methods 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
229960000541 cetyl alcohol Drugs 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000011109 contamination Methods 0.000 description 1
238000010924 continuous production Methods 0.000 description 1
230000008021 deposition Effects 0.000 description 1
LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
239000012969 di-tertiary-butyl peroxide Substances 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
CWINGZLCRSDKCL-UHFFFAOYSA-N ethoxycarbonyloxy ethyl carbonate Chemical compound CCOC(=O)OOC(=O)OCC CWINGZLCRSDKCL-UHFFFAOYSA-N 0.000 description 1
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
238000001914 filtration Methods 0.000 description 1
XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
239000007792 gaseous phase Substances 0.000 description 1
210000004907 gland Anatomy 0.000 description 1
239000003292 glue Substances 0.000 description 1
239000003979 granulating agent Substances 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
238000012544 monitoring process Methods 0.000 description 1
229920005615 natural polymer Polymers 0.000 description 1
231100000989 no adverse effect Toxicity 0.000 description 1
229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
238000010422 painting Methods 0.000 description 1
HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
125000005634 peroxydicarbonate group Chemical group 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920001291 polyvinyl halide Polymers 0.000 description 1
BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000012744 reinforcing agent Substances 0.000 description 1
239000011369 resultant mixture Substances 0.000 description 1
235000019515 salmon Nutrition 0.000 description 1
238000007790 scraping Methods 0.000 description 1
238000010008 shearing Methods 0.000 description 1
239000004208 shellac Substances 0.000 description 1
ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
229940113147 shellac Drugs 0.000 description 1
235000013874 shellac Nutrition 0.000 description 1
DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
239000007779 soft material Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
229920002803 thermoplastic polyurethane Polymers 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
229960004418 trolamine Drugs 0.000 description 1
239000002383 tung oil Substances 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F14/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
- C08F14/02—Monomers containing chlorine
- C08F14/04—Monomers containing two carbon atoms
- C08F14/06—Vinyl chloride
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/002—Scale prevention in a polymerisation reactor or its auxiliary parts
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/002—Scale prevention in a polymerisation reactor or its auxiliary parts
- C08F2/004—Scale prevention in a polymerisation reactor or its auxiliary parts by a prior coating on the reactor walls

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Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Polymerisation Methods In General (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CA298,530A 1977-03-08 1978-03-08 Vinyl halide polymerization in internally cooled reactor Expired CA1085094A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
AUPC932477		1977-03-08
AUPC.9324		1977-03-08

Publications (1)

Publication Number	Publication Date
CA1085094A true CA1085094A (en)	1980-09-02

Family

ID=3766925

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA298,530A Expired CA1085094A (en)	1977-03-08	1978-03-08	Vinyl halide polymerization in internally cooled reactor

Country Status (13)

Country	Link
US (1)	US4220743A (it)
JP (1)	JPS53130784A (it)
AT (1)	AT365614B (it)
BE (1)	BE864650A (it)
CA (1)	CA1085094A (it)
DE (1)	DE2810097C2 (it)
ES (1)	ES467657A1 (it)
GB (1)	GB1597292A (it)
IT (1)	IT1174360B (it)
NL (1)	NL7802523A (it)
PT (1)	PT67750A (it)
SE (1)	SE439639B (it)
ZA (1)	ZA781291B (it)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ZA794091B (en) *	1978-08-29	1980-10-29	Ici Ltd	New epoxy resin and use as build-up suppressant coating in polymerisation reactors and in vinyl halide polymerisations
US4297320A (en) *	1979-04-30	1981-10-27	The B. F. Goodrich Company	Coating polymerization reactors with the reaction products of thiodiphenols and a bleach
JPS578207A (en) *	1980-06-17	1982-01-16	Tokuyama Sekisui Kogyo Kk	Suspension polymerization of vinyl chloride
JPS6030681B2 (ja) *	1981-03-23	1985-07-18	信越化学工業株式会社	エチレン性二重結合を有する単量体の重合方法
US4355141A (en) *	1981-05-20	1982-10-19	Mitsui Toatsu Chemical, Inc.	Polymerizing vinyl chloride in reactor treated with condensates
JPS6037122B2 (ja) *	1982-08-27	1985-08-24	徳山積水工業株式会社	重合容器に付着したスケ−ルを除去する方法
US4517344A (en) *	1982-10-12	1985-05-14	Kanegafuchi Kagaku Kogyo Kabushiki Kaisha	Process for polymerization of acrylate or methacrylate
US4466905A (en) *	1983-04-11	1984-08-21	Cosden Technology, Inc.	Polymerization inhibition process for vinyl aromatic compounds
US4468343A (en) *	1983-04-11	1984-08-28	Cosden Technology, Inc.	Polymerization co-inhibitors for vinyl aromatic compounds
IT1190641B (it) *	1986-05-16	1988-02-16	Enichem Polimeri	Procedimento per la polimerizzazione in sospensione acquosa di monomeri vinilici contenenti alogeno
KR100191378B1 (ko) *	1989-09-18	1999-06-15	후루타 다케시	비닐 클로라이드 수지를 제조하기위한 미세현탁중합법
ES2097255T3 (es) *	1991-10-21	1997-04-01	Shinetsu Chemical Co	Agente de prevencion de costra de polimero.
JPH05230111A (ja) *	1992-02-20	1993-09-07	Shin Etsu Chem Co Ltd	重合体スケール付着防止剤、重合体スケールの付着を防止する重合器及びそれを使用する重合体製造方法
JP2678703B2 (ja) *	1992-02-20	1997-11-17	信越化学工業株式会社	重合体スケール付着防止剤及びそれを利用する重合体の製造方法
JPH05230112A (ja) *	1992-02-24	1993-09-07	Shin Etsu Chem Co Ltd	重合体スケール付着防止剤、重合体スケールの付着を防止する重合器及びそれを使用する重合体製造方法
JPH05320210A (ja) *	1992-05-21	1993-12-03	Shin Etsu Chem Co Ltd	重合体スケール付着防止剤ならびに重合体スケールの付着を防止する重合器及び重合体の製造方法
JPH0680707A (ja) *	1992-08-28	1994-03-22	Shin Etsu Chem Co Ltd	重合体スケール付着防止剤、重合体スケールの付着を防止する重合器及びそれを使用する重合体製造方法
CA2097570A1 (en) *	1992-06-04	1993-12-05	Toshihide Shimizu	Polymer scale preventive agent
EP1198481B1 (en)	1999-07-14	2006-01-04	Johnson Polymer, Inc.	Process for the continuous production of epoxy - (meth)acrylic - styrene polymers and their use in coating
US6605681B1 (en)	2000-07-12	2003-08-12	Johnson Polymer, Inc.	Process for the continuous production of epoxylated addition polymers, and powder and liquid coating applications containing epoxylated addition polymers

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US1955731A (en) *	1926-11-11	1934-04-24	Bakelite Corp	Phenol resin and process of making the same
US3440196A (en) *	1966-05-05	1969-04-22	Gen Electric	Coating solutions and methods for preparing and using the same
DE91560C (it) *	1970-05-07
US3778423A (en) *	1971-06-28	1973-12-11	Universal Pvc Resins	Method for reducing polymer deposit in polymerization of vinyl chloride
US4024330A (en) *	1975-04-08	1977-05-17	The B. F. Goodrich Company	Internally coated reaction vessel and process for coating the same
CA1064785A (en) *	1974-09-18	1979-10-23	B.F. Goodrich Company (The)	Internally coated reaction vessel and process for coating the same
JPS5153589A (en) *	1974-11-06	1976-05-12	Shinetsu Chemical Co	Harogenkabiniruno kaijojugoho
US4024301A (en) *	1975-05-02	1977-05-17	The B. F. Goodrich Company	Internally coated reaction vessel for use in olefinic polymerization
JPS5213592A (en) *	1975-07-23	1977-02-01	Shin Etsu Chem Co Ltd	Polymerization of vinyl chloride
JPS5941443B2 (ja) *	1976-07-30	1984-10-06	信越化学工業株式会社	重合体の製造方法

1978
- 1978-03-02 US US05/882,926 patent/US4220743A/en not_active Expired - Lifetime
- 1978-03-06 ZA ZA00781291A patent/ZA781291B/xx unknown
- 1978-03-07 JP JP2506878A patent/JPS53130784A/ja active Granted
- 1978-03-07 PT PT67750A patent/PT67750A/pt unknown
- 1978-03-07 BE BE185737A patent/BE864650A/xx not_active IP Right Cessation
- 1978-03-07 SE SE7802577A patent/SE439639B/xx unknown
- 1978-03-07 IT IT20963/78A patent/IT1174360B/it active
- 1978-03-08 NL NL7802523A patent/NL7802523A/xx not_active Application Discontinuation
- 1978-03-08 DE DE2810097A patent/DE2810097C2/de not_active Expired
- 1978-03-08 CA CA298,530A patent/CA1085094A/en not_active Expired
- 1978-03-08 GB GB9181/78A patent/GB1597292A/en not_active Expired
- 1978-03-08 AT AT0166278A patent/AT365614B/de not_active IP Right Cessation
- 1978-03-08 ES ES467657A patent/ES467657A1/es not_active Expired

Also Published As

Publication number	Publication date
SE439639B (sv)	1985-06-24
US4220743A (en)	1980-09-02
ZA781291B (en)	1979-04-25
ES467657A1 (es)	1978-10-16
GB1597292A (en)	1981-09-03
DE2810097C2 (de)	1982-05-06
PT67750A (en)	1978-04-01
IT7820963A0 (it)	1978-03-07
JPS53130784A (en)	1978-11-15
IT1174360B (it)	1987-07-01
SE7802577L (sv)	1978-09-09
JPS571528B2 (it)	1982-01-12
AT365614B (de)	1982-02-10
BE864650A (fr)	1978-09-07
DE2810097A1 (de)	1978-09-21
ATA166278A (de)	1981-06-15
NL7802523A (nl)	1978-09-12

Legal Events

Date	Code	Title	Description
1997-09-02	MKEX	Expiry

Publication	Publication Date	Title
CA1085094A (en)	1980-09-02	Vinyl halide polymerization in internally cooled reactor
US4391960A (en)	1983-07-05	Process for the polymerization of vinyl halide polymers
CA1189236A (en)	1985-06-18	Vinyl chloride polymerisation process
US4255470A (en)	1981-03-10	Process for preventing polymer buildup in a polymerization reactor
US4256863A (en)	1981-03-17	Vinyl halide polymerization process, reactor therefor and coating product for use in process and with reactor
US4181787A (en)	1980-01-01	Vinyl halide polymerization process and reactor therefor
CA2138182C (en)	1996-11-12	Polymerization process of vinyl chloride
US4076951A (en)	1978-02-28	Method of polymerizing vinyl chloride
US4359560A (en)	1982-11-16	Method for reducing wall fouling in vinyl chloride polymerization
CA1102490A (en)	1981-06-02	Process for the manufacture of vinyl chloride polymers
GB1578805A (en)	1980-11-12	Vinyl halide polymerisation process and reactor and coating composition
US4464516A (en)	1984-08-07	Process for preparing vinyl chloride polymers
US4451625A (en)	1984-05-29	Reduction of wall fouling in the suspension polymerization of vinyl chloride homopolymer
US4659791A (en)	1987-04-21	Internally coated reaction vessel for use in olefinic polymerization
GB2029844A (en)	1980-03-26	Polyethyleneimine derivative for suppressing build-up in vinyl halide polymerization reactors
US4588613A (en)	1986-05-13	Process for reducing polymer buildup
NO153372B (no)	1985-11-25	Fremgangsmaate for polymerisering av vinylklorid.
KR810001790B1 (ko)	1981-11-14	비닐 할라이드 단량체의 중합방법
EP0000430A1 (en)	1979-01-24	Vinyl halide polymerization process
US4585842A (en)	1986-04-29	Method of treating a polymerizing reactor
US4719089A (en)	1988-01-12	Internally coated reaction vessel for use in olefinic polymerization
EP0027691B1 (en)	1983-10-12	Vinyl chloride polymerisation process
NO751555L (it)	1975-11-04
GB1576597A (en)	1980-10-08	Process for the polymerisation or copolymerisation of halogenated vinyl monomers in aqueous suspension ormicrosuspension
JP2821697B2 (ja)	1998-11-05	塩化ビニル系重合体の製造法